McEvoy Aisling M, Langford Aili V, Liau Shin J, Goordeen Darshna, Reeve Emily, Turner Justin P
Centre for Medicine Use and Safety, Monash Institute of Pharmaceutical Sciences, Parkville, Victoria, Australia.
Faculty of Medicine and Health, Sydney Pharmacy School, The University of Sydney, Camperdown, New South Wales, Australia.
J Am Geriatr Soc. 2025 Sep;73(9):2905-2913. doi: 10.1111/jgs.19512. Epub 2025 May 7.
Benzodiazepine receptor agonists (BZRAs) (benzodiazepines and z-drugs) may provide limited benefits in the management of insomnia when used short-term. However, they increase the risk of harms including falls, fractures, hospitalizations, and cognitive impairment. Deprescribing (cessation) of BZRAs may be beneficial for older adults and people living with cognitive impairment as they are at heightened risk of adverse events. This review investigated the effects of patient-directed, non-pharmacological interventions to support deprescribing of BZRAs used for insomnia in older adults and people living with cognitive impairment.
Embase, CENTRAL, Scopus, and Medline were searched in January 2024 with no publication date restrictions. Screening, data extraction, and risk of bias assessments (ROB2 for randomized studies, ROBINS-I for non-randomized studies) were conducted independently by two authors. Outcomes of interest included the proportion of participants who ceased BZRAs, reduction in BZRAs, switching to another medication, sleep outcomes, and clinical outcomes. Studies were included if they investigated BZRA deprescribing in older adults (≥ 65 years) or people living with cognitive impairment.
Seventeen reports analyzing 16 studies in hospital, community, and aged care settings were included. BZRA cessation rates ranged between 23% to 72% for written education (n = 6); 14% to 57% for combined written and verbal education (n = 5); and 9% to 100% for multi-component interventions (n = 6). One report investigated a BZRA deprescribing educational intervention in people with cognitive impairment and found comparable effectiveness to participants without cognitive impairment. Most studies were at a high risk of bias.
Patient-directed interventions led to BZRA cessation, although there was significant variability between studies. It is unknown if all interventions examined are similarly effective for people living with cognitive impairment. Further research investigating approaches to deprescribing BZRAs in older adults or people with cognitive impairment is required.
苯二氮䓬受体激动剂(BZRAs)(苯二氮䓬类药物和Z类药物)短期使用时在失眠管理中可能仅提供有限益处。然而,它们会增加跌倒、骨折、住院和认知障碍等危害风险。停用BZRAs可能对老年人和认知障碍患者有益,因为他们发生不良事件的风险更高。本综述调查了以患者为导向的非药物干预措施对支持停用用于老年人和认知障碍患者失眠治疗的BZRAs的效果。
2024年1月检索了Embase、CENTRAL、Scopus和Medline,无出版日期限制。由两位作者独立进行筛选、数据提取和偏倚风险评估(随机研究采用ROB2,非随机研究采用ROBINS-I)。感兴趣的结局包括停用BZRAs的参与者比例、BZRAs的减少、换用另一种药物、睡眠结局和临床结局。如果研究调查了老年人(≥65岁)或认知障碍患者停用BZRA的情况,则纳入研究。
纳入了17篇分析医院、社区和老年护理环境中16项研究的报告。书面教育的BZRA停药率在23%至72%之间(n = 6);书面和口头教育相结合的停药率在14%至57%之间(n = 5);多成分干预的停药率在9%至100%之间(n = 6)。一份报告调查了针对认知障碍患者的BZRA停药教育干预措施,发现其效果与无认知障碍的参与者相当。大多数研究存在高偏倚风险。
以患者为导向的干预措施导致了BZRA停药,尽管各研究之间存在显著差异。尚不清楚所有研究的干预措施对认知障碍患者是否同样有效。需要进一步研究调查老年人或认知障碍患者停用BZRAs的方法。